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rs863223787

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223787(G;T)
Make rs863223787(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position114398721
GeneTBX5
is asnp
is mentioned by
dbSNPrs863223787
ebirs863223787
HLIrs863223787
Exacrs863223787
Varsomers863223787
Maprs863223787
PheGenIrs863223787
hapmaprs863223787
1000 genomesrs863223787
hgdprs863223787
ensemblrs863223787
gopubmedrs863223787
geneviewrs863223787
scholarrs863223787
googlers863223787
pharmgkbrs863223787
gwascentralrs863223787
openSNPrs863223787
23andMers863223787
23andMe allrs863223787
SNP Nexus

SNPshotrs863223787
SNPdbers863223787
MSV3drs863223787
GWAS Ctlgrs863223787
Max Magnitude0
ClinVar
Risk rs863223787(T;T)
Alt rs863223787(T;T)
Reference rs863223787(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TBX5
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.114836526C>A
CLNSRC
CLNACC RCV000199799.1,